"Linkage Disequilibrium" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Nonrandom association of linked genes. This is the tendency of the alleles of two separate but already linked loci to be found together more frequently than would be expected by chance alone.
Descriptor ID |
D015810
|
MeSH Number(s) |
G05.348.500
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Concept/Terms |
Linkage Disequilibrium- Linkage Disequilibrium
- Disequilibrium, Linkage
- Disequilibriums, Linkage
- Linkage Disequilibriums
|
Below are MeSH descriptors whose meaning is more general than "Linkage Disequilibrium".
Below are MeSH descriptors whose meaning is more specific than "Linkage Disequilibrium".
This graph shows the total number of publications written about "Linkage Disequilibrium" by people in this website by year, and whether "Linkage Disequilibrium" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1996 | 0 | 1 | 1 |
2001 | 1 | 0 | 1 |
2004 | 0 | 1 | 1 |
2005 | 0 | 1 | 1 |
2006 | 1 | 1 | 2 |
2007 | 0 | 2 | 2 |
2008 | 0 | 1 | 1 |
2009 | 0 | 1 | 1 |
2010 | 0 | 1 | 1 |
2011 | 0 | 3 | 3 |
2012 | 0 | 3 | 3 |
2013 | 0 | 1 | 1 |
2014 | 0 | 1 | 1 |
2016 | 0 | 1 | 1 |
2017 | 1 | 24 | 25 |
2018 | 1 | 13 | 14 |
2019 | 1 | 2 | 3 |
2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Linkage Disequilibrium" by people in Profiles.
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Detection of Phenotype-Related Mutations of COVID-19 via the Whole Genomic Data. IEEE/ACM Trans Comput Biol Bioinform. 2021 Jul-Aug; 18(4):1242-1249.
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SARS-CoV-2: Possible recombination and emergence of potentially more virulent strains. PLoS One. 2021; 16(5):e0251368.
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An atlas connecting shared genetic architecture of human diseases and molecular phenotypes provides insight into COVID-19 susceptibility. Genome Med. 2021 05 17; 13(1):83.
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Functional alterations caused by mutations reflect evolutionary trends of SARS-CoV-2. Brief Bioinform. 2021 03 22; 22(2):1442-1450.
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Rapid Spread of Mutant Alleles in Worldwide SARS-CoV-2 Strains Revealed by Genome-Wide Single Nucleotide Polymorphism and Variation Analysis. Genome Biol Evol. 2021 02 03; 13(2).
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Modifiable lifestyle factors and severe COVID-19 risk: a Mendelian randomisation study. BMC Med Genomics. 2021 02 03; 14(1):38.
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Host genetic effects in pneumonia. Am J Hum Genet. 2021 01 07; 108(1):194-201.
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Variant analysis of 1,040 SARS-CoV-2 genomes. PLoS One. 2020; 15(11):e0241535.
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The major genetic risk factor for severe COVID-19 is inherited from Neanderthals. Nature. 2020 11; 587(7835):610-612.
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Most frequent South Asian haplotypes of ACE2 share identity by descent with East Eurasian populations. PLoS One. 2020; 15(9):e0238255.